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COVID-19 pandemic has made it increasingly difficult for ECS progastrin to ensure clinical research is maintained.
As a result, the sponsor made the decision to end patient enrollment prematurely.
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| Name | Class |
|---|---|
| Centre Hospitalier Princesse Grace | OTHER |
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Dosage of progastrin in asymptomatic person participating in colon cancer screening
For anyone who will participate in colon screening at the Princess Grace Hospital of Monaco and who has signed the informed consent document. A blood test will be performed in addition to the screening test to assess the rate of progastrin.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| progastrin | Other | anyone who will participate in colon screening at the Princess Grace Hospital in Monaco and who has signed the informed consent document |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| progastrin | Diagnostic Test | PROCODE is an interventional study of category 2 (non-medicinal product), with a minimal risks and restrictions, involving only one blood drawn at the screening of colon cancer. |
| Measure | Description | Time Frame |
|---|---|---|
| progastrin rate | measuring the rate of progastrin in the blood | from 15 days to 2 months (until results are obtained) |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Georges GARNIER | Centre Hospitalier Princesse Grace | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Centre Hospitalier Princesse Grace, Monaco | Montpellier | MC | 34070 MONTPELLIER | France |
Monocentric study; No IPD sharing
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Interventional Research, at Risk and Minimal Constraints, Category 2
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